Papers associated with upper blastopore lip (and sia1)

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	Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula., Ding Y., Dev Biol. June 15, 2017; 426 (2): 176-187.
	Identification of new regulators of embryonic patterning and morphogenesis in Xenopus gastrulae by RNA sequencing., Popov IK., Dev Biol. June 15, 2017; 426 (2): 429-441.
	A gradient of maternal Bicaudal-C controls vertebrate embryogenesis via translational repression of mRNAs encoding cell fate regulators., Park S., Development. March 1, 2016; 143 (5): 864-71.
	Specification of anteroposterior axis by combinatorial signaling during Xenopus development., Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
	Identification of microRNAs and microRNA targets in Xenopus gastrulae: The role of miR-26 in the regulation of Smad1., Liu C., Dev Biol. January 1, 2016; 409 (1): 26-38.
	NF2/Merlin is required for the axial pattern formation in the Xenopus laevis embryo., Zhu X., Mech Dev. November 1, 2015; 138 Pt 3 305-12.
	Xenopus Pkdcc1 and Pkdcc2 Are Two New Tyrosine Kinases Involved in the Regulation of JNK Dependent Wnt/PCP Signaling Pathway., Vitorino M., PLoS One. August 13, 2015; 10 (8): e0135504.
	Early neural ectodermal genes are activated by Siamois and Twin during blastula stages., Klein SL., Genesis. May 1, 2015; 53 (5): 308-20.
	Direct regulation of siamois by VegT is required for axis formation in Xenopus embryo., Li HY., Int J Dev Biol. January 1, 2015; 59 (10-12): 443-51.
	The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling., Iwasaki Y., Development. October 1, 2014; 141 (19): 3740-51.
	Symmetry breakage in the vertebrate embryo: when does it happen and how does it work?, Blum M., Dev Biol. September 1, 2014; 393 (1): 109-23.
	Maternal syntabulin is required for dorsal axis formation and is a germ plasm component in Xenopus., Colozza G., Differentiation. July 1, 2014; 88 (1): 17-26.
	Maternal Dead-End1 is required for vegetal cortical microtubule assembly during Xenopus axis specification., Mei W., Development. June 1, 2013; 140 (11): 2334-44.
	Klf4 is required for germ-layer differentiation and body axis patterning during Xenopus embryogenesis., Cao Q., Development. November 1, 2012; 139 (21): 3950-61.
	Maternal Mga is required for Wnt signaling and organizer formation in the early Xenopus embryo., Gu F., Acta Biochim Biophys Sin (Shanghai). November 1, 2012; 44 (11): 939-47.
	Transcriptional integration of Wnt and Nodal pathways in establishment of the Spemann organizer., Reid CD., Dev Biol. August 15, 2012; 368 (2): 231-41.
	Subfunctionalization and neofunctionalization of vertebrate Lef/Tcf transcription factors., Klingel S., Dev Biol. August 1, 2012; 368 (1): 44-53.
	Dynamic in vivo binding of transcription factors to cis-regulatory modules of cer and gsc in the stepwise formation of the Spemann-Mangold organizer., Sudou N., Development. May 1, 2012; 139 (9): 1651-61.
	Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ., Dev Biol. January 15, 2012; 361 (2): 220-31.
	mNanog possesses dorsal mesoderm-inducing ability by modulating both BMP and Activin/nodal signaling in Xenopus ectodermal cells., Miyazaki A., PLoS One. January 1, 2012; 7 (10): e46630.
	Cortical rotation and messenger RNA localization in Xenopus axis formation., Houston DW., Wiley Interdiscip Rev Dev Biol. January 1, 2012; 1 (3): 371-88.
	The functions of maternal Dishevelled 2 and 3 in the early Xenopus embryo., Tadjuidje E., Dev Dyn. July 1, 2011; 240 (7): 1727-36.
	Siamois and Twin are redundant and essential in formation of the Spemann organizer., Bae S., Dev Biol. April 15, 2011; 352 (2): 367-81.
	A gene regulatory network controlling hhex transcription in the anterior endoderm of the organizer., Rankin SA, Rankin SA., Dev Biol. March 15, 2011; 351 (2): 297-310.
	Protein tyrosine kinase 7 has a conserved role in Wnt/β-catenin canonical signalling., Puppo F., EMBO Rep. January 1, 2011; 12 (1): 43-9.
	Yes-associated protein 65 (YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone., Gee ST., PLoS One. January 1, 2011; 6 (6): e20309.
	beta-Catenin primes organizer gene expression by recruiting a histone H3 arginine 8 methyltransferase, Prmt2., Blythe SA., Dev Cell. August 17, 2010; 19 (2): 220-31.
	Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.
	Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1., Louie SH., PLoS One. January 1, 2009; 4 (2): e4310.
	A p38 MAPK-CREB pathway functions to pattern mesoderm in Xenopus., Keren A., Dev Biol. October 1, 2008; 322 (1): 86-94.
	Lrig3 regulates neural crest formation in Xenopus by modulating Fgf and Wnt signaling pathways., Zhao H., Development. April 1, 2008; 135 (7): 1283-93.
	Expression of Siamois and Twin in the blastula Chordin/Noggin signaling center is required for brain formation in Xenopus laevis embryos., Ishibashi H., Mech Dev. January 1, 2008; 125 (1-2): 58-66.
	The Xenopus Nieuwkoop center and Spemann-Mangold organizer share molecular components and a requirement for maternal Wnt activity., Vonica A., Dev Biol. December 1, 2007; 312 (1): 90-102.
	Wise retained in the endoplasmic reticulum inhibits Wnt signaling by reducing cell surface LRP6., Guidato S., Dev Biol. October 15, 2007; 310 (2): 250-63.
	Wnt11/beta-catenin signaling in both oocytes and early embryos acts through LRP6-mediated regulation of axin., Kofron M., Development. February 1, 2007; 134 (3): 503-13.
	Maternal XTcf1 and XTcf4 have distinct roles in regulating Wnt target genes., Standley HJ., Dev Biol. January 15, 2006; 289 (2): 318-28.
	SOX7 and SOX18 are essential for cardiogenesis in Xenopus., Zhang C., Dev Dyn. December 1, 2005; 234 (4): 878-91.
	XIC is required for Siamois activity and dorsoanterior development., Snider L., Mol Cell Biol. June 1, 2005; 25 (12): 5061-72.
	Depletion of three BMP antagonists from Spemann's organizer leads to a catastrophic loss of dorsal structures., Khokha MK., Dev Cell. March 1, 2005; 8 (3): 401-11.
	New roles for FoxH1 in patterning the early embryo., Kofron M., Development. October 1, 2004; 131 (20): 5065-78.
	The involvement of Frodo in TCF-dependent signaling and neural tissue development., Hikasa H., Development. October 1, 2004; 131 (19): 4725-34.
	Analysis of Spemann organizer formation in Xenopus embryos by cDNA macroarrays., Wessely O., Dev Biol. May 15, 2004; 269 (2): 552-66.
	Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus., Kuroda H., PLoS Biol. May 1, 2004; 2 (5): E92.
	PKC delta is essential for Dishevelled function in a noncanonical Wnt pathway that regulates Xenopus convergent extension movements., Kinoshita N., Genes Dev. July 1, 2003; 17 (13): 1663-76.
	Flamingo, a cadherin-type receptor involved in the Drosophila planar polarity pathway, can block signaling via the canonical wnt pathway in Xenopus laevis., Morgan R., Int J Dev Biol. May 1, 2003; 47 (4): 245-52.
	Molecular link in the sequential induction of the Spemann organizer: direct activation of the cerberus gene by Xlim-1, Xotx2, Mix.1, and Siamois, immediately downstream from Nodal and Wnt signaling., Yamamoto S., Dev Biol. May 1, 2003; 257 (1): 190-204.
	Repression of organizer genes in dorsal and ventral Xenopus cells mediated by maternal XTcf3., Houston DW., Development. September 1, 2002; 129 (17): 4015-25.
	The competence of marginal zone cells to become Spemann's organizer is controlled by Xcad2., Levy V., Dev Biol. August 1, 2002; 248 (1): 40-51.
	otx2 expression in the ectoderm activates anterior neural determination and is required for Xenopus cement gland formation., Gammill LS., Dev Biol. December 1, 2001; 240 (1): 223-36.
	Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis., Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.

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